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Updated: May 5, 2026

Translational Orthotopic Models of Glioblastoma Multiforme
Published on: February 17, 2023
Is there pseudoprogression in secondary glioblastomas?
Tareq A Juratli1, Kay Engellandt, Tim Lautenschlaeger
1Department of Neurosurgery, University Hospital Carl Gustav Carus, Technical University of Dresden, Dresden, Germany.
Pseudoprogression (PP) is rare in secondary glioblastoma (sGBM) patients treated with chemoradiation therapy. This finding suggests differences in PP incidence between primary and secondary glioblastoma.
Area of Science:
- Neuro-oncology
- Radiation Oncology
- Medical Genetics
Background:
- Pseudoprogression (PP) is a common challenge in glioblastoma (GBM) treatment.
- Data on PP incidence in secondary glioblastomas (sGBM) is limited compared to primary GBM.
- Understanding PP in sGBM is crucial for accurate treatment assessment.
Purpose of the Study:
- To evaluate the frequency of pseudoprogression (PP) in adult patients with secondary glioblastomas (sGBM).
- To investigate potential associations between PP and MGMT promoter methylation, IDH mutations, or 1p/19q codeletion in sGBM.
- To compare PP incidence in sGBM with known rates in primary GBM.
Main Methods:
- Retrospective analysis of adult sGBM patients receiving chemoradiation therapy (CRTx) with temozolomide (TMZ).
- Assessment of PP using Response Assessment in Neuro-Oncology (RANO) criteria.
- Correlation analysis with MGMT promoter methylation, IDH mutations, and 1p/19q codeletion status.
Main Results:
- No pseudoprogression (PP) was observed in any of the 15 evaluable sGBM patients.
- PP did not occur in patients receiving concomitant or sequential CRTx with TMZ, regardless of MGMT or IDH status.
- Median follow-up was 3.4 years, with a median overall survival of 18.2 months.
Conclusions:
- The incidence of pseudoprogression (PP) appears very low in secondary glioblastomas (sGBM) treated with chemoradiation.
- MGMT promoter methylation and IDH mutations did not correlate with PP in this sGBM cohort.
- Findings highlight distinct patterns of PP between primary and secondary glioblastomas.
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